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Structure of 13675-94-0
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4-Chloro-6-nitroquinoline is a heterocyclic compound featuring a chlorine atom at the 4-position and a nitro group at the 6-position of the quinoline scaffold. This electron-deficient architecture enhances reactivity in cross-coupling processes and facilitates incorporation into pharmaceutical intermediates requiring polar, aromatic frameworks. The molecule exhibits bench-stable handling characteristics and compatibility with diverse synthetic transformations under standard conditions.
4-Chloro-6-nitroquinoline serves as a versatile building block in medicinal chemistry, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. Its orthogonal reactivity profile—where the chlorine site undergoes selective substitution while the nitro group remains intact—facilitates the construction of complex quinoline-based scaffolds. The compound exhibits good bench stability and is amenable to standard purification techniques, making it well-suited for high-throughput synthesis and process-scale applications.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: